HOXD10 M319K mutation in a family with isolated congenital vertical talus

Journal of Orthopaedic Research

Volumn 24, Issue 3, 2006, Pages 448-453

  Dobbs, Matthew B ^a,b   Gurnett, Christina A ^a   Pierce, Brandon ^a   Exner, G Ulrich ^g   Robarge, Jason ^a   Morcuende, Jose A ^c   Cole, William G ^d   Templeton, Peter A ^e   Foster, Bruce ^f   Bowcock, Anne M ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b SHRINERS HOSPITAL FOR CHILDREN   (United States)

^c UNIVERSITY OF IOWA   (United States)

^d HOSPITAL FOR SICK CHILDREN   (Canada)

^e LEEDS GENERAL INFIRMARY   (United Kingdom)

^f UNIVERSITY OF ADELAIDE   (Australia)

^g UNIVERSITY OF ZURICH   (Switzerland)

Author keywords

Congenital vertical talus; Gene mutation; HOXD10

Indexed keywords

DNA; HOMEODOMAIN PROTEIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR HOXD; UNCLASSIFIED DRUG; HOXD10 PROTEIN, HUMAN;

ARTICLE; CHROMOSOME 2Q; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; CLUBFOOT; CONGENITAL FLATFOOT; CONTROLLED STUDY; DNA ISOLATION; FOOT MALFORMATION; GENE CLUSTER; GENETIC HETEROGENEITY; GENETIC RISK; GENETIC VARIABILITY; HUMAN; LINKAGE ANALYSIS; MISSENSE MUTATION; MUTATIONAL ANALYSIS; PEDIGREE ANALYSIS; PRIORITY JOURNAL; RISK ASSESSMENT; CAUCASIAN; CHROMOSOME 2; CONGENITAL MALFORMATION; FEMALE; GENETIC LINKAGE; GENETIC PREDISPOSITION; GENETICS; MALE; METABOLISM; NUCLEOTIDE SEQUENCE; PEDIGREE; TALUS;

CHROMOSOMES, HUMAN, PAIR 2; DNA MUTATIONAL ANALYSIS; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; FOOT DEFORMITIES, CONGENITAL; GENETIC PREDISPOSITION TO DISEASE; HOMEODOMAIN PROTEINS; HUMANS; LINKAGE (GENETICS); MALE; MUTATION, MISSENSE; PEDIGREE; TALUS; TRANSCRIPTION FACTORS;

EID: 33645728813     PISSN: 07360266     EISSN: None     Source Type: Journal    
DOI: 10.1002/jor.20052     Document Type: Article

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